Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGGGGGCCCAATGGGAGGAAGGCC[A/C]GGGGGCCGAGGAGCACCAGCGGTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 300392 | ||||||||||||||||||||
Literature Links: |
WAS PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
WAS - Wiskott-Aldrich syndrome | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000377.2 | 92 | Silent Mutation | CCA,CCC | P,P 10 | NP_000368.1 | |
XM_011543977.2 | 92 | Silent Mutation | CCA,CCC | P,P 10 | XP_011542279.1 | |
XM_017029786.1 | 92 | Silent Mutation | CCA,CCC | P,P 10 | XP_016885275.1 |